Linked Data
dbSNP Id:
rs1555768180
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.47003916_47003917insTGCA , CM000681.2:g.47003916_47003917insTGCA | GRCh38 |
| NC_000019.9:g.47507173_47507174insTGCA , CM000681.1:g.47507173_47507174insTGCA | GRCh37 |
| NC_000019.8:g.52199013_52199014insTGCA | NCBI36 |
| NG_047014.1:g.90350_90351insTGCA | |
| NG_047014.2:g.147920_147921insTGCA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000404338.8:c.7728_7729insTGCA | ENSP00000385720.2:n.7728_7729insTGCA | |
| ENST00000672722.1:c.*3228_*3229insTGCA MANE Select | ENSP00000500409.1:n.*3228_*3229insTGCA | |
| ENST00000404338.7:c.7728_7729insTGCA | ENSP00000385720.2:n.7728_7729insTGCA | |
| ENST00000614079.1:c.7305_7306insTGCA | ENSP00000483730.1:n.7305_7306insTGCA | |
| NM_004491.4:c.7728_7729insTGCA | NP_004482.4:n.7728_7729insTGCA | |
| NM_004491.5:c.*3228_*3229insTGCA MANE Select | NP_004482.4:n.*3228_*3229insTGCA |